Herndon, VA, March 14, 2013 --(PR.com
)-- Acceliant is looking forward to meet participants at the BioPharma Asia Convention being held in Singapore from 18 to 21 March. Visit Booth #D24 to know about its comprehensive eClinical Suite, and pick a free copy of white paper on ‘EDC Migration for In-flight Trials’, and ‘EDC and e-PRO Integration’.
Speaking on the participation, Santhosh S. Nagaraj, Sales Head, said, "We will demonstrate Acceliant’s proprietary integrated e-Patient Reported Outcomes (e-PRO) and Electronic Data Capture (EDC) system, which eliminates the integration overhead; UTB and other clinical trial management modules that drive efficiency. We are also excited to explore partnership opportunities with the leaders from Asia and around the world.”
“BioPharma Asia will be a great platform for us to showcase how our products can help manage data through all the phases of clinical trials, speed up trials, reduce costs, and drive efficiency,” added Prashant Bhavaraju, CMO.
About Acceliant eClinical Suite
Acceliant eClinical Suite is competitive in meeting the challenges of today’s dynamic market conditions. The suite is a pre-eminent offering that continues its 12-year history of providing innovative solutions for the life sciences industry. The eClinical Suite is a robust, scalable, and flexible. It has been proven by more than 350 Phase I-IV trials, covering all therapeutic areas and medical device trials. Engineered for agility, our service model differentiators enable us to implement and deploy in response to the data, functional, and analytic needs of clinical trials.